L59W (p.Leu59Trp) variant of PLK1 (P53350)
L59W (p.Leu59Trp) in PLK1 (P53350) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
L59W (p.Leu59Trp) variant details
- p.Leu59Trp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available